Journal
INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH
Volume 59, Issue 30, Pages 13420-13427Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acs.iecr.0c00366
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Funding
- National Natural Science Foundation of China [21776076]
- Fundamental Research Funds for the Central Universities [WA1817013]
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Framework aluminum (Al-F) has a correlative relationship with the acid sites in a zeolite, which has been regarded as the key point during the adsorption behavior in alkylation of benzene with methanol. Here, the Al-F distribution in HZSM-5 channels was successfully controlled by different pore-filling agents and organic structure-directing agents (OSDAs) in the synthesis step. HZSM-5 samples with Al-F preferentially located in the intersections and sinusoidal/straight channels were synthesized using tetrapropylammonium hydroxide and pentaerythritol with Na cations as an OSDA and a pore-filling agent, respectively. Catalytic performances in alkylation of benzene with methanol showed that HZSM-5 zeolite with Al-F sitting in the channel and channel intersections generated a coadsorption effect yielding higher benzene conversion, xylene selectivity, and catalytic stability in this reaction. Meanwhile, HZSM-5 zeolite with more Al-F located particularly in the sinusoidal channel exhibited better shape selectivity to the para-xylene product.
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